Alchene Flashcards

1
Q

Metode de obtinere

A
  1. Eliminarea apei din alcool
  2. Eliminarea hidracizilor din halogenuri de alchil
  3. Eliminarea halogenurilor din compusii dihalogenati vicinali
  4. Decarboxilarea ac nesaturati
  5. Dehidrogenarea alcanilor
  6. Descompunerea termica a alcanilor
  7. Descompunerea esterilor alcoolilor cu diversi acizi
  8. Izomerizarea alchenelor
  9. Degradarea bazelor cuaternare de amoniu
  10. Descompunerea sulfoxizilor\sulfonelor
  11. Scindarea eterilor
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2
Q

Eliminarea apei din alcool

A

CH3-CH2-OH > CH2=CH2 + H2O

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3
Q

Eliminarea halogenilor din compusii dihalogenati vicinali

A

BrCH2-CH2Br + Zn > CH2=CH2 + ZnBr2

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4
Q

Decarboxilarea ac nesaturati

A

R-CH=CH-COOH > CO2 + R-CH=CH2

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5
Q

Dehidrogenarea alcanilor

A

CH3-CH2-CH2-CH3 > CH3-CH=CH-CH3 + H2
Se foloseste Cr2O3 + Al2O3 la temperatura

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6
Q

Descompunerea termica a alcanilor

A

Cracare si piroliza

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7
Q

Descompunerea esterilor alcoolilor cu diversi acizi

A

RCH2CH2OCOCH3 > RCH=CH2 + CH3COOH
Temperatura 300-600

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8
Q

Izomerizarea alchenelor

A

CH2=CH-CH2-CH3 > CH3-CH=CH-CH3 > CH3-C=CH2 SI IN IZO

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9
Q

Degradarea bazelor cuaternare de amoniu

A

[(CH3-CH3)4N]+OH- > [CH3-CH2-OH] + (C2H5)3N > CH2=CH2 +H2O

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10
Q

Descompunerea sulfoxizilor si sulfonelor

A

SULFOXID > ALCHENA
SULFONA > ALCHENA

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11
Q

Scindarea eterilor

A

R’-O-CH2CH2R ——R”Li—> RCH=CH2 + R’OLi + R”H

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12
Q

PROPRIETATI CHIMICE

A

A. Aditie
1. Hidrogenare
2. Aditia halogenilor
3. Aditia hidracizilor
4. Tratare cu solutii diluate de clor\brom
5. Acid sulfuric
6. Oxidul de azot si clorura de nitrozil
7. Ac carboxilici
8. Apa
B. Oxidare
I. La dubla legatura
1. Oxidare blanda
2. Degradare oxidativa sau oxidare energica
3. Epoxilare
4. Ozon
II. Ardere
C. Substitutie in poz alilica
1. Autooxidarea
2. Halogenarea
D. Polimerizare

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13
Q

Aditie. Hidrogenare

A

CH2=CH2 + H2 > CH3-CH3

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14
Q

ADITIA HALOGENILOR

A

CH2=CH2 + Br2 > BRCH2-CH2BR

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15
Q

ADITIA HIDRACIZILOR

A

CH2=CH2 + HI > CH3-CH2I

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16
Q

TRATARE CU SOL DE CLOR\BROM

A

CH2=CH2 + HOCL > CLCH2-CH2OH

17
Q

ADITIA ACIDILUI SULFURIC

A

CH2=CH2 + HOSO3H > CH3-CH2-OSO3H

18
Q

ADITIA APEI

A

CH2=CH-CH3 + H2O > CH3-CH-CH3 IN IZO OH

19
Q

ADITIA AC CARBOXILICI

A

CH2=C(CH3) + RCOOH > RCOOC(CH3)3

20
Q

OXIDARE BLANDA

A

R-CH=CH-R +[O] + H20 > R-CH-CH-R OH LA C DIN LEG DUBLA
SE FACE CU PERMANGANAT

21
Q

OXIDARE ENERGICA

A

C ———-> CETONA
CH ———> COOH
CH2 ———> CO2 + H20
SE FACE CU BICROMAT + H2SO4

22
Q

EPOXILARE

A

R-CH=CH-R + [O] > R-CH-CH-R O LEGAT DE AMBII C
SE FOLOSESTE AG2O LA 120 GRADE

23
Q

OZON

A

CH3-CH=CH2 + O3 +H2O > CH3-CH=O + CH2=O

24
Q

ARDERE

A

CO2 + H2O

25
Q

SUBSTITUTIE. AUTOOXIDARE

A

C-C-C=C + O2 > C-C-C=C IN POZ ALILICA O-O-H

26
Q

HALOGENARE IN POZ ALILICA

A

C=C-C + X2 > C=C-CH2X + HX
LA 400-600 GRADE

27
Q

POLIMERIZARE

A

nH2C=CH-R > (-CH2-CH-)n R LA CH